| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66002120-66002245 | Rare:36; Clinvar:2 | ||||
| chr11:71448385-71448652 | Common:1; Rare:64 | ||||
| chr11:74949102-74949279 | Common:4; Rare:44 | ||||
| chr11:88337714-88337892 | Common:3; Rare:82; Clinvar:3; Clinvar (benign):2 | ||||
| chr11:119018378-119018550 | Common:4; Rare:63 | ||||
| chr11:124673716-124673935 | Common:4; Rare:64 | ||||
| chr11:126268875-126269157 | Rare:97; Clinvar:1 | ||||
| chr12:6970648-6970919 | Common:2; Rare:79 | ||||
| chr12:42326092-42326197 | Rare:28 | ||||
| chr12:112013155-112013452 | Common:1; Rare:98 | ||||
| chr12:123233137-123233481 | Common:2; Rare:105; Clinvar:1 | ||||
| chr14:20455051-20455259 | Common:2; Rare:61 | ||||
| chr14:24232330-24232465 | Common:6; Rare:31 | ||||
| chr14:49620596-49620776 | Common:2; Rare:55 | ||||
| chr14:60981019-60981268 | Rare:97 |